Cleared Traditional

K913464 - STOMAVISION (STV)

K913464 is an FDA 510(k) clearance for STOMAVISION (STV), manufactured by Trophy Radiologie. The device is a Class 1 Dental device with product code EIA cleared through the Traditional 510(k) pathway after a 100-day FDA review.

K913464 · Trophy Radiologie · Dental device
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Nov 1991
Decision
100d
Days
Class 1
Risk

K913464 is an FDA 510(k) clearance for the STOMAVISION (STV). Classified as Unit, Operative Dental (product code EIA), Class I - General Controls.

Submitted by Trophy Radiologie (Vincennes, Cedex (Paris), FR). The FDA issued a Cleared decision on November 13, 1991 after a review of 100 days - within the typical 510(k) review window.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.6640 - the FDA dental device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Dental review framework, consistent with the majority of Class II 510(k) submissions.

View all Trophy Radiologie devices

FDA 510(k) Submission Details - K913464

510(k) Number K913464 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 05, 1991
Decision Date November 13, 1991
Days to Decision 100 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
27d faster than avg
Panel avg: 127d · This submission: 100d
Pathway characteristics
Predicate-based equivalence.

EIA Device Classification - Class 1, General Controls

Product Code EIA Unit, Operative Dental
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.6640
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - EIA Unit, Operative Dental

All 101
Devices cleared under the same product code (EIA) and FDA review panel - the closest regulatory comparables to K913464.
A-DEC 2612 ASSISTANT'S CART
K933163 · A-Dec, Inc. · Oct 1993
A-DEC 3131 DUO WALLMOUNT (WITH INSTRUMENTATION)
K933165 · A-Dec, Inc. · Oct 1993
A-DEC 3127 ASSISTANT'S WALLMOUNT
K933168 · A-Dec, Inc. · Oct 1993
MDT/CASTLE PURUS DENTAL UNIT
K914697 · Mdt Corp., Inc. · Nov 1991
ASEPTIMINI UNIT, ADU-10
K905401 · Aseptico, Inc. · Feb 1991
ORAL PHARYNGEAL CLEANSING DEVICE
K905011 · Concord/Portex · Jan 1991